IADR Abstract Archives

In-situ Erosion Study of a 0.454% Stannous Fluoride Dentifrice

Objective: To compare the anti-erosion benefits of two marketed dentifrices in a 15 day in situ model.

Method: The present study utilized a single centre, double blind, randomised, two-treatment, and four period crossover design. Thirty-seven subjects were enrolled and 33 completed the study. Each study period took place over a span of 15 days. Subjects were randomized to treatment sequences and received one of two marketed dentifrice products each period. Treatments included a 0.454% Stannous Fluoride dentifrice (Oral-B PRO EXPERT®) and a 0.3% Triclosan/sodium fluoride dentifrice (Colgate Total Advanced®). Subjects wore an intra-oral appliance retaining 2 polished human enamel samples for 6 hours/day, swishing with the assigned dentifrice slurry twice a day and swishing with 250ml of orange juice for 10 minutes four times/ day. Contact profilometry was used to measure surface changes of enamel samples at Baseline, days 10 and 15. Two measurements for each sample were recorded at each visit.

Result: No statistically significant treatment differences were observed at Baseline for the two dentifrice groups (p>0.44) with means of -0.015 and -0.024 for the Stannous Fluoride and the Triclosan dentifrices, respectively. At day 10 the Stannous Fluoride dentifrice demonstrated 66.8% lower enamel loss than the Triclosan dentifrice (p<0.0001) with means of 1.222µm and 3.676 µm, respectively, and at day 15, a 68.3% lower enamel loss (p<0.0001) with means of 1.595 µm and 5.027 µm, respectively. Both test products were well tolerated.

Conclusion: The in situ clinical study demonstrated the superior anti-erosion efficacy of the 0.454% Stannous Fluoride dentifrice relative to the 0.3% Triclosan/sodium fluoride dentifrice against an erosive challenge to human enamel.

Division: AADR/CADR Annual Meeting
Meeting: 2014 AADR/CADR Annual Meeting (Charlotte, North Carolina)
Location: Charlotte, North Carolina
Year: 2014
Final Presentation ID: 571
Abstract Category|Abstract Category(s): Oral Health Research
Authors
  • West, Nicola  ( Periodontology, Clinical Trials Unit, University of Bristol, Bristol, , England )
  • Hellin, Nikki  ( Periodontology, Clinical Trials Unit, University of Bristol, Bristol, , England )
  • Macdonald, Emma  ( Periodontology, Clinical Trials Unit, University of Bristol, Bristol, , England )
  • Seong, Joon  ( University of Bristol, Bristol, , England )
  • Biesbrock, Aaron R.  ( Procter & Gamble Company, Mason, OH, USA )
  • Barker, M.  ( Procter & Gamble Company, Mason, OH, USA )
  • He, Tao  ( Procter & Gamble Company, Mason, OH, USA )
  • SESSION INFORMATION
    Poster Session
    Safety and Efficacy Methods for Evaluation of Oral Care Products
    03/20/2014